中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Pharmaco-proteogenomic characterization of liver cancer organoids for precision oncology

文献类型:期刊论文

作者Ji, Shuyi1,2; Feng, Li3; Fu, Zile2; Wu, Gaohua2; Wu, Yingcheng2; Lin, Youpei2; Lu, Dayun4,5; Song, Yuanli4,5; Cui, Peng6; Yang, Zijian2
刊名SCIENCE TRANSLATIONAL MEDICINE
出版日期2023-07-26
卷号15期号:706页码:15
ISSN号1946-6234
DOI10.1126/scitranslmed.adg3358
通讯作者Zhou, Hu(gaoqiang@fudan.edu.cn) ; Sun, Yidi(ydsun@ion.ac.cn) ; Gao, Qiang(zhouhu@simm.ac.cn)
英文摘要Organoid models have the potential to recapitulate the biological and pharmacotypic features of parental tumors. Nevertheless, integrative pharmaco-proteogenomics analysis for drug response features and biomarker investigation for precision therapy of patients with liver cancer are still lacking. We established a patient-derived liver cancer organoid biobank (LICOB) that comprehensively represents the histological and molecular characteristics of various liver cancer types as determined by multiomics profiling, including genomic, epigenomic, transcriptomic, and proteomic analysis. Proteogenomic profiling of LICOB identified proliferative and metabolic organoid subtypes linked to patient prognosis. High-throughput drug screening revealed distinct response patterns of each subtype that were associated with specific multiomics signatures. Through integrative analyses of LICOB pharmaco-proteogenomics data, we identified the molecular features associated with drug responses and predicted potential drug combinations for personalized patient treatment. The synergistic inhibition effect of mTOR inhibitor temsirolimus and the multitargeted tyrosine kinase inhibitor lenvatinib was validated in organoids and patient-derived xenografts models. We also provide a user-friendly web portal to help serve the biomedical research community. Our study is a rich resource for investigation of liver cancer biology and pharmacological dependencies and may help enable functional precision medicine.
WOS关键词HEPATOCELLULAR-CARCINOMA ; SENSITIVITY ; ACTIVATION ; PATHWAY ; HGF
WOS研究方向Cell Biology ; Research & Experimental Medicine
语种英语
出版者AMER ASSOC ADVANCEMENT SCIENCE
WOS记录号WOS:001037244900001
源URL[http://119.78.100.183/handle/2S10ELR8/306911]  
专题中国科学院上海药物研究所
通讯作者Zhou, Hu; Sun, Yidi; Gao, Qiang
作者单位1.Fudan Univ, Jinshan Hosp, Ctr Tumor Diag & Therapy, Shanghai 201508, Peoples R China
2.Fudan Univ, Key Lab Carcinogenesis & Canc Invas, Dept Liver Surg & Transplantat, Liver Canc Inst,Zhongshan Hosp,Minist Educ, Shanghai 200032, Peoples R China
3.Chinese Acad Sci, Inst Neurosci, CAS Ctr Excellence Brain Sci & Intelligence Techn, Shanghai 200031, Peoples R China
4.Chinese Acad Sci, Dept Analyt Chem, Shanghai 201203, Peoples R China
5.Chinese Acad Sci, Shanghai Inst Mat Med, CAS Key Lab Receptor Res, Shanghai 201203, Peoples R China
6.Burning Rock Biotech, Shanghai 201114, Peoples R China
7.D1 Med Technol, Shanghai 200235, Peoples R China
8.Chinese Acad Sci, Inst Pasteur Shanghai, Key Lab Mol Virol & Immunol, Shanghai 200031, Peoples R China
9.Fudan Univ, Shanghai Canc Ctr, Dept Radiat Oncol, Shanghai 200032, Peoples R China
10.Fudan Univ, Shanghai Canc Ctr, Canc Inst, Shanghai 200032, Peoples R China
推荐引用方式
GB/T 7714
Ji, Shuyi,Feng, Li,Fu, Zile,et al. Pharmaco-proteogenomic characterization of liver cancer organoids for precision oncology[J]. SCIENCE TRANSLATIONAL MEDICINE,2023,15(706):15.
APA Ji, Shuyi.,Feng, Li.,Fu, Zile.,Wu, Gaohua.,Wu, Yingcheng.,...&Gao, Qiang.(2023).Pharmaco-proteogenomic characterization of liver cancer organoids for precision oncology.SCIENCE TRANSLATIONAL MEDICINE,15(706),15.
MLA Ji, Shuyi,et al."Pharmaco-proteogenomic characterization of liver cancer organoids for precision oncology".SCIENCE TRANSLATIONAL MEDICINE 15.706(2023):15.

入库方式: OAI收割

来源:上海药物研究所

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